NM_007315.4:c.185C>G

HGVS Expressions

  • NG_008294.1:g.10200C>G
  • NM_007315.4:c.185C>G
  • NP_009330.1:p.Ser62Ter
  • NC_000002.12:g.191009051G>C
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CTGA Clinical Significance

Pathogenic

Variant Type

Substitution

Epidemiology in the Arab World

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Subject IDCountry of OriginAllele CountAllele FrequencyCTGA Clinical Significance Condition(s)ReferenceRemarks
613796.4.1Saudi Arabia2PathogenicImmunodeficiency 31BLe Voyer et al. 2021
613796.4.2Saudi Arabia1Le Voyer et al. 2021 Father of 613796.4.1
613796.4.3Saudi Arabia1Le Voyer et al. 2021 Mother of 613796.4.1
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